Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:88856929-88857143 | Common:4; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
chr16:89657673-89657849 | Rare:89 | ||||
chr16:89686635-89686706 | Common:5; Rare:46 | ||||
chr17:2303776-2303983 | Common:2; Rare:76 | ||||
chr17:2336441-2336528 | Rare:31 | ||||
chr17:3668576-3668799 | Common:1; Rare:82 | ||||
chr17:4807006-4807181 | Common:3; Rare:59 | ||||
chr17:4939915-4940092 | Common:1; Rare:57 | ||||
chr17:6640690-6641037 | Common:6; Rare:90 | ||||
chr17:7012335-7012654 | Rare:108 | ||||
chr17:7219826-7219961 | Common:3; Rare:64; Clinvar:5; Clinvar (benign):2 | ||||
chr17:7242299-7242606 | Common:1; Rare:104 | ||||
chr17:7251963-7252215 | Rare:96 | ||||
chr17:7484235-7484366 | Common:1; Rare:50 | ||||
chr17:7583736-7583858 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):3 |